Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.38421078T>G	CA224450	OTC	c.1061T>G (p.Phe354Cys) c.172-245043T>G (n.172-245043T>G)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
X	g.38421078T=	CA2424888125	OTC	c.1061T= (p.Phe354=) c.172-245043T= (n.172-245043T=)	dbSNP

Number of alleles fetched